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Amlodipine Besylate and Benazepril Hydrochloride

NDC 82868-041 · Northwind Health Company, LLC

Generic nameAmlodipine Besylate and Benazepril Hydrochloride
Dosage formCAPSULE
RouteORAL
Active ingredient(s)AMLODIPINE BESYLATE, BENAZEPRIL HYDROCHLORIDE
Strength10; 20 mg/1; mg/1
Pharmacologic classAngiotensin Converting Enzyme Inhibitor [EPC], Angiotensin-converting Enzyme Inhibitors [MoA], Calcium Channel Antagonists [MoA], Calcium Channel Blocker [EPC], Cytochrome P450 3A Inhibitors [MoA], Decreased Blood Pressure [PE], Dihydropyridine Calcium Channel Blocker [EPC], Dihydropyridines [CS]
Marketing categoryANDA

Packages

82868-041-90 — 90 CAPSULE in 1 BOTTLE, PLASTIC (82868-041-90)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

81279-134 — amlodipine, 81279-135 — amlodipine, 82009-026 — AMLODIPINE BESYLATE, 82009-027 — AMLODIPINE BESYLATE, 82009-028 — AMLODIPINE BESYLATE, 82804-164 — Amlodipine Besylate, 82804-297 — Amlodipine besylate, 82804-969 — AMLODIPINE BESYLATE, 82804-970 — AMLODIPINE BESYLATE, 82804-971 — AMLODIPINE BESYLATE, 82868-031 — Amlodipine Besylate, 82868-089 — Benazepril Hydrochloride, 83008-035 — Amlodipine Besylate, 83209-399 — Amlodipine Besylate, 84386-100 — Benazepril Hydrochloride, 84386-101 — Benazepril Hydrochloride, 84386-102 — Benazepril Hydrochloride, 84677-013 — Amlodipine and Benazepril Hydrochloride, 87441-016 — Amlodipine besylate, 87441-017 — Amlodipine besylate, +624 more

From the FDA National Drug Code Directory, retrieved August 24, 2026. Product listings are submitted by labelers; FDA does not verify them.

Read from: FDA National Drug Code Directory, product.txt and package.txt (accessdata.fda.gov/cder/ndctext.zip) — Snapshot retrieved 2026-08-24, loaded 2026-08-24; CMS Medicare Part B Drug Average Sales Price (ASP) Pricing Files (cms.gov/medicare/payment/part-b-drugs/asp-pricing-files) -- the NDC-HCPCS crosswalk and Part B payment limit files — 2026 Q3 (July 2026 release). All data sources · How to read the labels